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Naslov Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy (Article)
Autori Dawod Phepy GA Jancic Jasna B  Marjanovic Ana  Marjanovic Ana  Jankovic Milena Z  Samardzic Janko M  Potkonjak Dario Djuric Vesna Mesaros Sarlota T Novakovic Ivana V  Abdel Motaleb Fayda I Kostic Vladimir S Nikolic Dejan P  
Info GENES, (2020), vol. 11 br. 9, str. -
Projekat Serbian Ministry of Education, Science and Technological Development [ON175090, ON175091, 200110]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov The influence of ANNK1/DRD2 haplotypes on the onset of complications of long-term levodopa therapy in Parkinson's disease (Meeting Abstract)
Autori Radojevic Branislava Dragasevic-Miskovic Natasa T Marjanovic Ana  Milovanovic Andona  Svetel Marina V  Petrovic Igor N Savic Miroslav M  Jancic Ivan R Kostic Vladimir K 
Info MOVEMENT DISORDERS, (2020), vol. 35 br. , Suppl. 1, str. S473-S474
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Yield of thePMP22deletion analysis in patients with compression neuropathies (Article)
Autori Ivanovic Vukan Marjanovic Ana  Bjelica Bogdan Kacar Aleksandra S Tubic Radoje M Jankovic Milena Z  Marjanovic Ana  Novakovic Ivana V  Rakocevic-Stojanovic Vidosava M Peric Stojan Z  
Info JOURNAL OF NEUROLOGY, (2020), vol. 267 br. 12, str. 3617-3623
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Neuropathic pain in patients with Charcot-Marie-Tooth type 1A (Article)
Autori Bjelica Bogdan Peric Stojan Z  Basta Ivana Z Bozovic Ivo Kacar Aleksandra S Marjanovic Ana  Ivanovic Vukan Marjanovic Ana  Jankovic Milena Z  Novakovic Ivana V  Rakocevic-Stojanovic Vidosava M 
Info NEUROLOGICAL SCIENCES, (2020), vol. 41 br. 3, str. 625-630
Projekat Ministarstvo Prosvete, Nauke i Tehnoloskog Razvoja [175083]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov GLUT1 deficiency syndrome: a case report with a novel SLC2A1 mutation (Article)
Autori Ivancevic Nikola  Cerovac Natasa M  Nikolic Blazo  Cuturilo Goran Marjanovic Ana  Marjanovic Ana  Novakovic Ivana V  
Info VOJNOSANITETSKI PREGLED, (2019), vol. 76 br. 5, str. 543-546
Projekat Serbian Ministry of Education, Science and Technological Development [ON175091]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy (Meeting Abstract)
Autori Dawod Phepy GA Rovcanin Branislav R  Marjanovic Ana  Marjanovic Ana  Jankovic Milena Z  Novakovic Ivana V  Motaleb Abdel F Jancic Jasna B  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1836-1837
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers (Meeting Abstract)
Autori Marjanovic Ana  Dobricic Valerija S Brankovic Marija  Jankovic Milena Z  Mandic Gorana B Stefanova Elka D  Stevic Zorica D Novakovic Ivana V  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 961-961
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov NOTCH3 mutations in Serbian CADASIL patients (Meeting Abstract)
Autori Jankovic Milena Z  Dobricic Valerija S Marjanovic Ana  Brankovic Marija  Pavlovic Aleksandra M  Dujmovic Irena Mijajlovic Milija D  Novakovic Ivana V  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 293-293
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: Firs experience (Meeting Abstract)
Autori Brankovic M Dobricic Valerija S Svetel Marina V  Peric Stojan Z  Stefanova Elka D  Marjanovic Ana  Petrovic Igor N Novakovic Ivana V  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 292-292
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy (Meeting Abstract)
Autori Dawod Phepy GA Rovcanin Branislav R  Marjanovic Ana  Marjanovic Ana  Jankovic Milena Z  Novakovic Ivana V  Dujmovic Irena Jancic Jasna B  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 181-181
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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